Amastin mRNA abundance in Trypanosoma cruzi is controlled by a 3 '-untranslated region position-dependent cis-element and an untranslated region-binding protein
Bc. Coughlin et al., Amastin mRNA abundance in Trypanosoma cruzi is controlled by a 3 '-untranslated region position-dependent cis-element and an untranslated region-binding protein, J BIOL CHEM, 275(16), 2000, pp. 12051-12060
The genome of Trypanosoma cruzi contains tandem arrays of alternating genes
encoding amastin and tuzin. Amastin is a surface glycoprotein abundantly e
xpressed on the intracellular mammalian amastigote form of the protozoan pa
rasite, and tuzin is a G-like protein. We demonstrated previously that the
amastin-tuzin gene cluster is polycistronically transcribed to an equal ext
ent in all parasite life cycle stages. The steady state level of amastin mR
NA, however, is 68-fold more abundant in amastigotes than in epimastigotes.
Here we show that the half-life of amastin mRNA is 7 times longer in amast
igotes than in epimastigotes. Linker replacement experiments demonstrate th
at the middle one-third of the 630-nucleotide 3'-untranslated region (UTR)
is responsible for the amastin mRNA up-regulation. This positive effect is
dependent on the distance of the 3'-UTR segment from the stop codon and the
polyadenylation site as well as on its orientation. A protein or protein c
omplex more abundant in amastigotes than in epimastigotes binds to this min
imally defined 3'-UTR segment and may be involved in its regulatory functio
n.